510(k) K152541 ยท NRY Catheter, Thrombus Retriever
Penumbra System ACE 64 and ACE 68 Reperfusion Catheters
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jan 13, 2016 |
| Received | Sep 4, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152541
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.